north york, on research participant study Jobs – 66 Openings This Week

Principal Investigator
MPA Recruitment Canada Ltd —Toronto, ON
- $350,000–$500,000 a year
- Full-time
- Medicine
- Doctoral degree
- In-person
- Dental care
- Paid time off
Quick apply
Senior Analyst, Real Estate Development
Fiera Capital —Toronto, ON
- $90,000–$110,000 a year
- Full-time
- Hybrid work
- Bilingual
- Microsoft Excel
- English
Research Coordinator II MAP UpstreamLab
Unity Health Toronto —Toronto, ON
- Full-time
- Bilingual
- English
- Research
10d
Research & Evaluation Assistant
YMCA of Greater Toronto —Toronto, ON
- $19.51 an hour
- Part-time
- Microsoft Outlook
- Microsoft Office
- Presentation skills
Quick apply
6d
Clinical Research Coordinator I
Centricity Research —Toronto, ON
- $50,000–$55,000 a year
- Full-time
- Bachelor's
- Designated paid holidays
- Dental care
Quick apply
Research Assistant - Anesthesia
WCH —Toronto, ON
- $27.08–$33.29 an hour
- Part-time
- Microsoft Word
- Microsoft Excel
- Microsoft Access
Quick apply
7d
Research Assistant Level 1
Baycrest —Toronto, ON
- $39,873–$54,826 a year
- Full-time
- Research
- Microsoft Office
- Databases
Research Assistant Level 2
Baycrest —Toronto, ON
- $26.29–$36.15 an hour
- Full-time
- Laboratory experience
- Research
- Master's degree
STEM Summer Camp Instructor (Online / In-person) (CAD/JAVA/HTML)
African Canadian Christian Network (ACCN) —North York, ON
- $20 an hour
- Temporary
- Hybrid work
- CAD
- Java
- JavaScript
Quick apply
Research Analyst - Institute for Mental Health Policy Research
CAMH —Toronto, ON
- $27.95–$37.28 an hour
- Part-time
- Data analysis skills
- Research
- Databases
3d
Clinical & Research Extern (Hybrid)
Michael Garron Hospital —Toronto, ON
- Temporary
- Nursing
- BLS Certification
- Research
Research Assistant 2 - Slaight Centre Research
CAMH —Toronto, ON
- $26.80–$33.05 an hour
- Full-time
- Microsoft Powerpoint
- Bilingual
- Microsoft Word
10d
Clinical Research Project Coordinator, Brain Tumor Research Centre
SickKids —Toronto, ON
- Temporary
- Microsoft Powerpoint
- Microsoft Word
- Research
2d
Research Assistant / Laboratory Specialist
Centricity Research —Vaughan, ON
- $21–$25 an hour
- Full-time
- Microsoft Office
- Designated paid holidays
- Dental care
Quick apply
Research Ethics Coordinator
OICR —Toronto, ON
- $70,000–$76,000 a year
- Hybrid work
- Microsoft Word
- Microsoft Excel
- Microsoft Outlook
CH&E Coordinator (Patient Engagement) - Clinical Research Services
CAMH —Toronto, ON
- $37.51–$50.60 an hour
- Full-time
- Bilingual
- English
- Research
1d
Clinical Research Project Coordinator-RI
SickKids —Toronto, ON
- Temporary
- Bachelor's
- Organizational skills
- Associate's degree
- Dental care
- Life insurance
7d
Sleep Technician (Casual)
Centricity Research —Toronto, ON
- $35–$45 an hour
- Part-time
- Flexible schedule
Quick apply
Research Coordinator - Shkaabe Makwa
CAMH —Toronto, ON
- $37.51–$50.60 an hour
- Full-time
- Bilingual
- Microsoft Word
- Microsoft Excel
7d
Research Coordinator
Baycrest —Toronto, ON
- $58,386–$72,983 a year
- Full-time
- Master's degree
- Bachelor's
- Psychology
6h

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research participant study jobs near north york, on

Principal Investigator

MPA Recruitment Canada Ltd -
Toronto, ON

Quick apply

Job details

Permanent | Full-time
$350,000–$500,000 a year

Qualifications

Medicine
Doctoral degree

Full job description

Principal Investigator
Toronto / Greater Toronto Area

MPA are retained by a Toronto based CRO to recruit for a Principal Investigator to join their team. The CRO run early-phase studies, bioequivalence testing, validate new drugs and provide regulatory support for pharmaceutical companies.

In this role, you will uphold Good Clinical Practice (GCP) by ensuring protocol compliance, protecting participant welfare, maintaining data integrity, and overseeing clinical investigations in line with regulatory requirements.

Duties and Responsibilities:

Conduct clinical trials in accordance with the approved protocol, including any amendments, as well as all study procedures and directives
Protect the rights, safety, and well-being of all participants, ensuring appropriate medical care throughout their involvement in the trial
Maintain thorough knowledge of investigational product(s) as outlined in the protocol, Investigator’s Brochure, and product monograph, and provide clear instructions to participants on proper use
Adhere to study randomization procedures and promptly document and report any premature unblinding to the sponsor and IRB, where applicable
Obtain and properly document informed consent in compliance with all regulatory and ethical requirements
Report all Serious Adverse Events (SAEs) and pregnancy notifications to the sponsor and IRB in a timely manner
Assess participant eligibility and ongoing health status, including medical history, inclusion/exclusion criteria, laboratory results, vital signs, adverse events, and study-specific procedures
Evaluate adverse events for causality, severity, and outcome, and recommend follow-up actions, including repeat testing when clinically indicated
Perform physical examinations of study participants
Confirm participant eligibility for investigational product administration
Follow up on clinically significant findings, including positive infectious disease results and notify appropriate health authorities as required
Ensure site compliance with Good Clinical Practice (GCP), standard operating procedures (SOPs), and applicable regulatory requirements
Review and sign clinical trial protocols, clinical study reports, and case report forms (as applicable), and participate in safety data reviews when required
Maintain accurate, complete, and legible study records, ensuring availability for review by monitors, auditors, and regulatory authorities.

Qualifications:

· Medical Doctor (M.D.) degree

· Registered and in good standing with CPSO.

· Minimum of 5 years of experience in clinical research

· At least 8 years of experience in drug development and clinical trial administration, with active clinical practice in a relevant therapeutic area

· Demonstrated ability to adapt to changing priorities and manage multiple projects effectively

· Advanced and up-to-date knowledge of:

o Clinical trials and study design

o Drug development processes

o Medical monitoring

o Applicable federal and international regulations and guidelines

· Familiarity with medical coding systems and adverse event review/reporting processes is considered an asset

Strong compensation package on offer. If this opportunity would be of interest to you, please reach out to [email protected] for a confidential chat.

Pay: $350,000.00-$500,000.00 per year

Benefits:

Dental care
Extended health care
Life insurance
Paid time off
Stock options

Work Location: In person

Quick apply

Refine Your Search

research participant study jobs in north york, on

Principal Investigator

Senior Analyst, Real Estate Development

Research Coordinator II MAP UpstreamLab

Research & Evaluation Assistant

Clinical Research Coordinator I

Research Assistant - Anesthesia

Research Assistant Level 1

Research Assistant Level 2

STEM Summer Camp Instructor (Online / In-person) (CAD/JAVA/HTML)

Research Analyst - Institute for Mental Health Policy Research

Clinical & Research Extern (Hybrid)

Research Assistant 2 - Slaight Centre Research

Clinical Research Project Coordinator, Brain Tumor Research Centre

Research Assistant / Laboratory Specialist

Research Ethics Coordinator

CH&E Coordinator (Patient Engagement) - Clinical Research Services

Clinical Research Project Coordinator-RI

Sleep Technician (Casual)

Research Coordinator - Shkaabe Makwa

Research Coordinator

I want to receive the latest job alerts for research participant study in north york, on

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